Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Development and Validation of Zero Absorbance Method for Simultaneous Estimation of Aliskiren and Amlodipine in Combined Dosage Form


Affiliations
1 School of Pharmacy, RK University, Rajkot, India
2 Shri Sarvajanik Pharmacy College, Mehsana, 384001, Gujarat, India
     

   Subscribe/Renew Journal


A simple, accurate, precise, economical and reproducible method was developed for simultaneous estimation of aliskiren and amlodipine in Combined Pharmaceutical Dosage Forms. The excipients in the commercial tablet preparation did not interfere with the assay. At 360 nm, Amlodipine showed some absorbance while aliskiren showed zero absorbance so that amlodipine was estimated at 360 nm. While at 287 nm aliskiren showed some absorbance while amlodipine showed zero absorbance so that aliskiren was estimated at 287nm. Linearity in concentration range of 10-120 μg/mL for aliskiren and 4-28 μg/mL for amlodipine with the mean recoveries were 100.08±1.32 and 99.76±1.05 % for aliskiren and amlodipine, respectively. Validation of the proposed method was carried out according to ICH guidelines. Thus the present study gives an excellent method for the determination of the two drugs in combined dosage formulation without their prior separation.

Keywords

Amlodipine Besylate, Aliskiren, Spectrophotometric Method.
Subscription Login to verify subscription
User
Notifications
Font Size


Abstract Views: 222

PDF Views: 0




  • Development and Validation of Zero Absorbance Method for Simultaneous Estimation of Aliskiren and Amlodipine in Combined Dosage Form

Abstract Views: 222  |  PDF Views: 0

Authors

R. Patel Samixa
School of Pharmacy, RK University, Rajkot, India
N. Patel Chhaganbhai
Shri Sarvajanik Pharmacy College, Mehsana, 384001, Gujarat, India

Abstract


A simple, accurate, precise, economical and reproducible method was developed for simultaneous estimation of aliskiren and amlodipine in Combined Pharmaceutical Dosage Forms. The excipients in the commercial tablet preparation did not interfere with the assay. At 360 nm, Amlodipine showed some absorbance while aliskiren showed zero absorbance so that amlodipine was estimated at 360 nm. While at 287 nm aliskiren showed some absorbance while amlodipine showed zero absorbance so that aliskiren was estimated at 287nm. Linearity in concentration range of 10-120 μg/mL for aliskiren and 4-28 μg/mL for amlodipine with the mean recoveries were 100.08±1.32 and 99.76±1.05 % for aliskiren and amlodipine, respectively. Validation of the proposed method was carried out according to ICH guidelines. Thus the present study gives an excellent method for the determination of the two drugs in combined dosage formulation without their prior separation.

Keywords


Amlodipine Besylate, Aliskiren, Spectrophotometric Method.